infancy electroclinical syndrome

electroclinical syndrome with onset in infancy occurring between birth and one year of age
MedicalCondition class_of_disease Q18553413
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infancy electroclinical syndrome

Summary

infancy electroclinical syndrome is a class of disease[1].

Key Facts

  • infancy electroclinical syndrome's instance of is recorded as class of disease[2].
  • infancy electroclinical syndrome is a type of electroclinical syndrome[3].
  • infancy electroclinical syndrome is a type of epilepsy syndrome[4].
  • infancy electroclinical syndrome is a type of epilepsy in children[5].
  • infancy electroclinical syndrome's genetic association is recorded as STXBP1[6].
  • infancy electroclinical syndrome's genetic association is recorded as DNM1[7].
  • infancy electroclinical syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050703[8].
  • infancy electroclinical syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050703[9].
  • infancy electroclinical syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_98258[10].
  • infancy electroclinical syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . Disease Ontology. Retrieved . wikidata.org.
  3. [4] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  6. [7] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  7. [8] . Disease Ontology. Retrieved . wikidata.org.
  8. [9] . Identifiers.org. ebi.ac.uk. Provenance: wikidata.org.
  9. [10] . wikidata.org.
  10. [11] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). infancy electroclinical syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/infancy-electroclinical-syndrome
MLA “infancy electroclinical syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/infancy-electroclinical-syndrome.
BibTeX @misc{4ortxyz_infancy-electroclinical-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{infancy electroclinical syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/infancy-electroclinical-syndrome}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): infancy electroclinical syndrome — https://4ort.xyz/entity/infancy-electroclinical-syndrome (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/infancy-electroclinical-syndrome · Last refreshed:

Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 28d ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    Imported from
    Umls cui C5681523
    Disease ontology id DOID:0050703
    Genetic association STXBP1, DNM1
    + 8 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39953|batch #39953]]: deprecate redundant disease superclasses (2)"
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